Acta geneticae medicae et gemellologiae: twin research: Volume 1 -

Acta geneticae medicae et gemellologiae: twin research

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Acta geneticae medicae et gemellologiae: twin research
ISSN: 0001-5660

EISSN: 2059-6324

URL: /core/journals/amg-acta-geneticae-medicae-et-gemellologiae-twin-research
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Acta geneticae medicae et gemellologiae: twin research

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Volume 1 - January 1952

Recensioni

T. Kemp. Arvehygiejne. Ejnar Munksgaard, Kobenhavn 1951.

Jan Mohr. Vitiligo in a pair of monovular Twins. Acta Genet, et Stat. Med. 2, 3. 1951.

A. Giordano. Enzimopenie ereditarie. Folia Hered. Path. vol. I, fasc. I (Luglio 1951).

W. Dölle. Bine weitere Ergänzung des Weilschen Diabetes - insipidus Stammbaumes. Ztschr. menschl. Vererb. u. Konstitutionslehre. 30, 3. 1951.

M. Lamy, C. Launay, M. Soulé. Dyslexie spécifique chez jumeaux identiques. La Semaine des Hopitaux. 28e année, n. 35 (1952).

N. Rossi. La poliposi ereditaria del crasso. Folia Hered. Path. vol. I, fasc. I. (Luglio 1951)

William G. Lennox. The heredity of epilepsy as told by relatives and twins. J.A.M.A. 146, pp. 529–536, giugno 1951.

C. J. Reitz. Rudimentêre occipitale arm. South African Medical Journal. Vol. 26, n. 15 (1952).

Walter Brenner. Zur Frage der Erblichkeit von Microcephalic und Hydrocephalie. Ztschr. menschl. Vererb. u. Konstitutionslehre. 30, 3. 375. 1951.

E. J. Gardner and H. P. Plenk. Hereditary Pattern for Multiple Osteomas in a Family Group. Am. J. Human Genet. Vol. 4, n. 1 (1952).

M. Zorzi. Le malformazioni diverticolari giganti del grosso intestino come fenomeno di gemellarità circoscritta. Folia Hered. Path. vol. I, fasc. I (Luglio 1951).

A. S. Wiener. Heredity of the M-N-S Blood Types. Theoretico-Statistical Considerations. Am. J. Human Genet. Vol. 4, n. 1 (1952).

I. Moretti. Confronto tra eritroolastosi fetale e sifilide congenita e loro comportamento nei gemelli. Folia Hered. Path, vol. I, fasc. II, (Ottobre 1951).

John W. Schut. Hereditary ataxia. Am. J. Human. Genetic. 3, 2, 93. 1951.

Charles Richet, Maurice Rymer et Jacqyes Besse. nanisme et infantilisme hypophysaires chez une hexadactyle héréditaire. La Semaine des Hopitaux, 27e Année, n. 53–54, 18–22 juillet 1951.

G. Pintus. Mutazione e somazione. Folia Hered. Path. vol. I fasc. II (Ottobre 1951).

L. Gedda. Psicologia e Linguaggio. Prolusione all’Anno Accademico 1951-1952. Istituto Universitario Maria SS. Assunta. Roma.

v. Verschuer, Otmar Frhr. Humangenetik körperliche Erbkranicheiten). Münch. med. Wschr. 49–51 (1951).

M. Ebnother. Ueber eme familiäre Skelettstörung mit multiloculären, aseptischen Knochennekrosen, insbesondere mit Osteochondrosis dissecans. Inaugural-Dissertation. Universität Zürich, 1952.

P. Brisotto. A proposito di un cancro del mesofaringe. Oto-rino-laringologia Italiana, vol. XIX, fasc. III. 1951.

Acta geneticae medicae et gemellologiae: twin research

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Volume 1 - January 1952

Recensioni